Evidence map›Paper›PMID 28645155›Full record

ArticleNucleic acids research2017

Features of genomic organization in a nucleotide-resolution molecular model of the Escherichia coli chromosome.

William C Hacker, Shuxiang Li, Adrian H Elcock

Abstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Physical models of bacterial chromosomes.Molecular microbiology · 2025
    Review
  2. Article
  3. Review
  4. Replicating Chromosomes in Whole-Cell Models of Bacteria.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  5. Integrative modeling of JCVI-Syn3A nucleoids with a modular approach.Current research in structural biology · 2024
    Article
  6. Article
  7. Dynamics of chromosome organization in a minimal bacterial cell.Frontiers in cell and developmental biology · 2023
    Article
  8. Review
  9. Review
  10. Building Structural Models of a Whole Mycoplasma Cell.Journal of molecular biology · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Art and Science of the Cellular Mesoscale.Trends in biochemical sciences · 2020
    Review
  15. Article
  16. Mesoscope: A Web-based Tool for Mesoscale Data Integration and Curation.MolVa : Workshop on Molecular Graphics and Visual Analysis of Molecular Data 2020 · 2020
    Article
  17. Article
  18. Article
  19. Whole-Cell Models and Simulations in Molecular Detail.Annual review of cell and developmental biology · 2019
    Review
  20. Transcription of Bacterial Chromatin.Journal of molecular biology · 2019
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

William C HackerDepartment of Biochemistry, University of Iowa, Iowa City, IA 52242, USA.
Shuxiang LiDepartment of Biochemistry, University of Iowa, Iowa City, IA 52242, USA.
Adrian H ElcockDepartment of Biochemistry, University of Iowa, Iowa City, IA 52242, USA.

Funding

Molecular Simulations of Folding & Association in Physiological EnvironmentsR01GM087290 · NIGMS · UNIVERSITY OF IOWA · PI ELCOCK, ADRIAN HAMILTON · 2009 to 2017
$1.6M
NIGMS NIH HHS R01 GM087290
6 · The paper itself

Abstract

We describe structural models of the Escherichia coli chromosome in which the positions of all 4.6 million nucleotides of each DNA strand are resolved. Models consistent with two basic chromosomal orientations, differing in their positioning of the origin of replication, have been constructed. In both types of model, the chromosome is partitioned into plectoneme-abundant and plectoneme-free regions, with plectoneme lengths and branching patterns matching experimental distributions, and with spatial distributions of highly-transcribed chromosomal regions matching recent experimental measurements of the distribution of RNA polymerases. Physical analysis of the models indicates that the effective persistence length of the DNA and relative contributions of twist and writhe to the chromosome's negative supercoiling are in good correspondence with experimental estimates. The models exhibit characteristics similar to those of 'fractal globules,' and even the most genomically-distant parts of the chromosome can be physically connected, through paths combining linear diffusion and inter-segmental transfer, by an average of only ∼10 000 bp. Finally, macrodomain structures and the spatial distributions of co-expressed genes are analyzed: the latter are shown to depend strongly on the overall orientation of the chromosome. We anticipate that the models will prove useful in exploring other static and dynamic features of the bacterial chromosome.

Indexed as

Genome, BacterialChromosomes, BacterialComputer SimulationDNA, BacterialEscherichia coliFractalsModels, GeneticModels, MolecularNucleic Acid ConformationOperonDNA, Bacterial

Identifiers

PMID28645155
PMCPMC5570083

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.